11 Clinical Data jobs in Pakistan

Research Associate, Clinical Trials Unit

Entity

Medical College Location

Introduction

Aga Khan University was established in 1983 as an international university with an objective to promote human welfare in general, and the welfare of the people in the countries in which it operates, by disseminating knowledge and providing instruction, training, research and service in the health sciences, education and such other branches of learning as the University may determine. As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment. Clinical Trials Unit (CTU) is a Department dedicated to develop a center of excellence for high quality and high impact clinical trials both nationally & internationally. The Department promotes AKU’s vision by providing leadership, consultation and facilitation in different phases of clinical trials in compliance with the International Standards and Good Clinical Practice (GCP) guidelines. This is a grant-funded contractual position. Responsibilities

You will be responsible to: liaise and coordinate study requirements with relevant units and departments of the institution, in line with AKU institutional policies organize and/or administer the informed consent process in conjunction with the Principal Investigator coordinate and provide patient care in compliance with protocol requirements specific to patients screening, recruitment, scheduling, and study visit procedures disburse investigational product upon written authorization from the PI and provide relevant teaching with respect to its administration maintain study documentation as per protocol and GCP requirements (screening, subject recruitment, investigational drug accountability, enrolment, monitoring and study visit, adverse/serious adverse events etc.) review/monitor patients for changes such as in health status, response to investigational product, adverse events, compliance in use of investigational product, concomitant medication use, protocol compliance provide laboratory support services including phlebotomy and collection/handling of required specimens (e.g. stool, urine, nasal swabs) using standard techniques review clinical trials protocols and shared feedback with supervisors for approval facilitate internal and external audits of the unit draft and report SAE, annual/periodic reports to regulatory bodies and sponsor Requirements

You should have: a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field must have a current registration & be in good standing with their professional association at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other possess excellent clinical skills ability to work in independently and versatility to work in a variety of roles excellent written and verbal communication skills in English integrity and strong research ethics efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel). a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field must have a current registration & be in good standing with their professional association at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other possess excellent clinical skills ability to work in independently and versatility to work in a variety of roles excellent written and verbal communication skills in English integrity and strong research ethics efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel). Comprehensive employment reference checks will be conducted. To Apply

Interested candidates should send their detailed CVs to and mark the subject line with position number "10011569". Only shortlisted candidates will be contacted. Applications should be submitted latest by

September 16, 2024

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JOB DESCRIPTION:

Minerva Research Solutions is a clinical trial management service provider.We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.

Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements.

We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.

Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.

Responsibilities:

• Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.
• Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations.
• Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.
• Provide ongoing compliance support including but not limited to:
• Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.
• Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).
• Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.
• Assist in preparing for all Sponsor and FDA audits.
• Assist in conducting internal audits to review key processes.
• Provide appropriate support to assigned cross-functional workgroups.
• Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.
• Query resolution and data entry and questionnaire preparation regarding the respective studies.
• Other related Quality Assurance projects as assigned.
• The QA Associate will report to the Quality Assurance Lead

Knowledge, Education, and Experience:

• Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc)with a keen interest in Clinical Research are strongly encouraged to apply.
• In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.
• Knowledge of IRB requirements.
• 1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred.
• Experience including external clinical/regulatory and document auditing will be a plus

Skills and Abilities:

• Good communication skills (interpersonal, written, verbal)
• Strong attention to detail and good time management skills
• Flexible attitude concerning work assignments
• Ability to manage multiple and varied tasks in a fast-moving environment
• Ability to interact professionally at all levels within the organization.
• Knowledge of the HIPAA Privacy Act and its application to clinical research.

Benefits:

• Competitive salary and performance-based bonuses.
• Medical health insurance coverage.
• Employees Old-age benefits coverage.
• Flexible work hours and remote work options.
• Professional learning and developmentsupport.
• Generous vacation and paid time off.
• Employee assistance programs for mental health.
• Company-sponsored events and team-building activities.
• Diverse, professional, and inclusive work environment.
• Opportunities for career growth.
• Cutting-edge technology and tools.
• Family-friendly policies, including parental leave.
• Commuter benefits or transportation assistance.
• Social responsibility and community involvement programs.

Openings:

04 positions
Full-time
On-site job

Work Schedule Timings:
Monday to Friday
Evening Shift (06 PM to 02 AM)
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)

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JOB DESCRIPTION:

Minerva Research Solutions is a clinical trial management service provider.We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle. Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements.

We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.

Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data. Responsibilities: Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness. Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations. Perform quality control checks; identify and track source documentation errors and non-conformances with requirements. Provide ongoing compliance support including but not limited to: Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans. Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs). Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities. Assist in preparing for all Sponsor and FDA audits. Assist in conducting internal audits to review key processes. Provide appropriate support to assigned cross-functional workgroups. Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement. Query resolution and data entry and questionnaire preparation regarding the respective studies. Other related Quality Assurance projects as assigned. The QA Associate will report to the Quality Assurance Lead Knowledge, Education, and Experience: Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc)with a keen interest in Clinical Research are strongly encouraged to apply. In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials. Knowledge of IRB requirements. 1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred. Experience including external clinical/regulatory and document auditing will be a plus Skills and Abilities: Good communication skills (interpersonal, written, verbal) Strong attention to detail and good time management skills Flexible attitude concerning work assignments Ability to manage multiple and varied tasks in a fast-moving environment Ability to interact professionally at all levels within the organization. Knowledge of the HIPAA Privacy Act and its application to clinical research. Benefits:

Competitive salary and performance-based bonuses. Medical health insurance coverage. Employees Old-age benefits coverage. Flexible work hours and remote work options. Professional learning and developmentsupport. Generous vacation and paid time off. Employee assistance programs for mental health. Company-sponsored events and team-building activities. Diverse, professional, and inclusive work environment. Opportunities for career growth. Cutting-edge technology and tools. Family-friendly policies, including parental leave. Commuter benefits or transportation assistance. Social responsibility and community involvement programs. Openings:

04 positions Full-time On-site job

Work Schedule Timings: Monday to Friday Evening Shift (06 PM to 02 AM) (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)

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Clinical Research Manager
BioVance Research International, Pakistan

BioVance Research International is seeking Clinical Research Monitors.

The designee will be responsible for managing the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Plans, oversees, and executes bioequivalence studies and PK studies. Oversees adherence to SOPs, Good Clinical Practice, and FDA/MHRA/EMA regulations.

The position reports directly to top management.

Package

Attractive gross salary offered.
Plus company medical scheme for self and family, company maintained car, and mobile SIM with monthly limit (all benefits after confirmation).
Probationary period: 3 months.

Job Specification

Requires a master's degree or PhD and at least 5 years of experience in the field or in a related area. Familiar with a variety of the field's concepts, practices, and procedures. Will need to rely on extensive experience and judgment to plan and accomplish goals. A degree of creativity and latitude is required and expected. Will perform a variety of tasks and lead and direct the work of others.

Information Technology and Services - Karachi, Pakistan

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Clinical Research Manager BioVance Research International, Pakistan

BioVance Research International is seeking Clinical Research Monitors.

The designee will be responsible for managing the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Plans, oversees, and executes bioequivalence studies and PK studies. Oversees adherence to SOPs, Good Clinical Practice, and FDA/MHRA/EMA regulations.

The position reports directly to top management. Package

Attractive gross salary offered. Plus company medical scheme for self and family, company maintained car, and mobile SIM with monthly limit (all benefits after confirmation). Probationary period: 3 months. Job Specification

Requires a master's degree or PhD and at least 5 years of experience in the field or in a related area. Familiar with a variety of the field's concepts, practices, and procedures. Will need to rely on extensive experience and judgment to plan and accomplish goals. A degree of creativity and latitude is required and expected. Will perform a variety of tasks and lead and direct the work of others. Information Technology and Services - Karachi, Pakistan

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Job Description :

Key Responsibilities :

• Organize, maintain, and update company databases
• Ensure accuracy, consistency, and security of data
• Develop and implement data management strategies
• Collaborate with cross-functional teams to support data needs
• Generate reports and insights to support business decisions
• Utilize tools such as Microsoft Word, Excel, and PowerPoint for documentation, analysis, and presentation

Job Specification :

• Minimum 2 years of hands-on experience in data management or a related field.
• Proficient in data tools and database systems.
• Strong attention to detail and analytical skills.
• Bachelor's degree in Computer Science, IT, Business, or a related field.

Job Rewards and Benefits : Medical #J-18808-Ljbffr

Job Description :

Key Responsibilities : Organize, maintain, and update company databases Ensure accuracy, consistency, and security of data Develop and implement data management strategies Collaborate with cross-functional teams to support data needs Generate reports and insights to support business decisions Utilize tools such as Microsoft Word, Excel, and PowerPoint for documentation, analysis, and presentation Job Specification :

Minimum 2 years of hands-on experience in data management or a related field. Proficient in data tools and database systems. Strong attention to detail and analytical skills. Bachelor's degree in Computer Science, IT, Business, or a related field. Job Rewards and Benefits : Medical #J-18808-Ljbffr

Data Management & Infrastructure Specialist About the job Data Management & Infrastructure Specialist

Expected Start Date: ASAP (position is open if you can still read this)

Positions Open: 05

Experience required: 0 to 2 years of working in a rapid startup environment

Education required: Education is flexible; however, a background in engineering is a plus

Salary package:

• Competitive salary and benefits package
• Monthly performance-based increments & cash bonuses
• Opportunity to work & grow with a Y-Combinator backed Founder whohas been doing startups for more than a decade
• More than 90% of customers are based in the USA (get exposure working on cutting-edge/disruptive tech)
• Opportunity to travel abroad and gain invaluable exposure
  • We have offices in Pakistan, Qatar & America.
  • Experience Hyper-growth in your career based on the Silicon Valley mindset
• High performance oriented and resilient work environment / workstation
• Company Issued Laptops/ Electronic Devices based on need and performance
• Free Food (Breakfast / Lunch / Dinner/ Snacks/ Fruits and Beverages)
• 24/7 Access to the office
• Performance base paid cool-off periods
• Dedicated time / Access to a plethora of Learning Resources
• Knowledge base mini library present at the office
• Fastest network (internet) in Pakistan
• Medical insurance, treatment and employee care for astronauts
• Overnight Stay Facilitation: Sleeping pods and Lockers
• Recreational activities / trips
• Highest Grade Massage Chairs
• Gaming corner - PS5
• Insured parking space
• Support team available for facilitation of employees
• Taxation, Accounts and legal assistance for the employees.
• The best work culture/team environment in the world! Primed to set you up for either running your own company or being a C-Level Executive in one.

Location

• This position requires you to travel Internationally to the MENA region and beyond if necessary.
• Based upon your exceptional performance, you might be assigned to work at one of our international bases.

About Cowlar

Cowlar is a venture-funded, Y-combinator start-up creating & delivering world-class engineering products and solutions in Retail, Industrial Automation, Enterprise Software, F&B, Internet of Things (IoT), Machine Learning, Robotics, Industry 4.0, and associated fields. Our exceptional team uses engineering best practices and a first-principles approach to solving complex problems and delivering enterprise-scale projects at warp speed.

With a culture that empowers big ideas and a focus on making our people the best version of themselves through continuous upskilling and enablement, we believe this is a place where exceptional talent comes together to make magic happen across multiple verticals. Were looking for like-minded people who understand our mission and are willing to become part of the journey.

Were looking for people who are not afraid of learning something new, who focus on hypergrowth, teach others what they have learnt and uphold the culture of the company. The ideal candidate should be self-driven and motivated. We want to work with people who realize their own potential and can execute quickly. We do not compromise on quality and your role should be to raise the bar and motivate others to be at their best.

Important Further Reading:

We value our culture above all else - Please go through this Culture Document carefully to understand our culture, values and what we represent.

To learn more about the type of work we have done.

About the Role:

We are seeking a detail-oriented Data Management and Infrastructure Specialist to oversee our
extensive video and image datasets crucial for computer vision model training. The ideal candidate will
ensure data integrity, accuracy, and real-time accessibility

Key Responsibilities:

Data Cleaning: Identify and remove corrupted or improperly cropped data, ensuring it iscorrectly re-extracted and validated.
Data Verification: Ensure video and image data align accurately with their labels and intendedpurposes. Correct any misalignments or discrepancies.
Frame Accuracy: Check and correct frame sequences within videos, ensuring no frames areout-of-order or missing.
Database Management: Maintain an accurate, up-to-date database with precise metadata,including video duration and relevant information, eliminating manual checks.
Pipeline Development: Build and manage efficient data pipelines that facilitate quick datasetcreation based on defined parameters and targeted output locations.
Real-Time Data Management: Continuously update and manage incoming data, ensuringdatasets remain current and immediately accessible.Collaboration with IT : Clearly communicate data and infrastructure requirements to the ITteam to ensure effective utilization and optimization of existing resources.
Backup Coordination: Work with the IT team to ensure regular backups, safeguarding dataintegrity and availability.

Required Skills:

1.Experience with data cleaning, verification, and management of video/image datasets.
2.Proficiency in database management and metadata handling.
3. Familiarity with developing automated pipelines for dataset generation.
4.Knowledge of data backup strategies and effective utilization of infrastructure.
5.Strong problem-solving abilities and attention to detail.

Preferred Qualifications:

1. Prior experience in computer vision or related AI/ML projects
2.Basic understanding of cloud infrastructure or high-performance storage solutions
3.Ability to automate workflows using scripting languages (Python, Bash, etc.)

• How to apply
  Visit work.cowlar.com and apply to the available position
  OR
  Email with Subject: (Your Name) - (Position)
  
  
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  We care less about years of experience and more about your drive, problem-solving skills, initiative, work ethic, personal integrity, and creativity. A primary requirement for this role is an extraordinary knack for clear and concise communication. You can demonstrate that knack by explaining why you think our company is a good match for you.

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Data Management Specialist - Remote
AutoScale Ventures, Pakistan

VinAudit.com Inc. is seeking a talented Data Management Specialist who will play an important role in executing important business data analysis and overseeing data production for quantitative and qualitative reports!

You would join a small team of 25 individuals working remotely and globally including in the Philippines, Pakistan, the United States, and Canada.

We specialize in vehicle data. Since 2011, we have aggregated billions of vehicle-related records, helped millions of consumers evaluate a car purchase, and served thousands of automotive businesses with access to our unique datasets.

We believe we're just getting started, and we'd love to explore how you could help.

Core Hours & Benefits:

• Location: Pakistan
• Core Hours: Monday - Friday, 9am - 5pm Seattle Time
• Base Pay : $3 USD/hr
• Benefits: HealthCare Coverage, Leave Days & Vacation Time, Paid Holidays, Equipment Funds

Job Specification

This role involves:

• Manage assigned tasks ensuring data meet the standard quality report
• Review pertinent data and build detailed reports for upper management
• Formulate techniques for quality data collection to ensure adequacy, accuracy and legitimacy of data
• Analyze and interpret large amounts of data
• Coordinate the production of data by the assigned department and by other data developers
• Field data-related questions and assist with client-support requests
• Organize documentation for recurring business processes
• Conduct in-depth web research on various topics
• Support and collaborate with various development tasks

Required experience:

• Strong organizational skills
• High-level verbal and written communication collaboration skills
• Detail-oriented with an eye for perfection
• Savvy with computers and familiar with modern, high-tech databases and IT systems
• Excellent understanding of data administration and management functions (collection, analysis, distribution etc.)
• Proficient at digesting, understanding, and analyzing large amounts of data and ability to translate complex problems clearly
• Review prepared data to ensure it is adequate, accurate, and complies with the standard requirements
• Consistently and independently productive with minimum supervision
• Passionate about self-development and continuous improvement

Resource Requirement:

• Stable internet connection (with a potential backup connection available)
• Available 100% exclusively (no other commitments)

Note: We aim to give our candidates the best experience possible. This means we will only get in touch if you have been shortlisted for the role. Thank you!

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